QA Specialist, Medical Devices (ISO 13485/MDR)
pEssilorLuxottica in Italy is seeking a QA Specialist to join the Quality Regulatory Affairs team and support the maintenance and continuous improvement of the Quality Management System, ensuring compliance with medical device requirements across the product lifecycle. /ppYou will collaborate with Production, RD, Regulatory Affairs and suppliers in a dynamic cross‑functional environment, drafting procedures, managing CAPAs, audits, and changes to sustain quality throughout the organization. /p #J-18808-Ljbffr